Canonical Allele Identifier: CA338920884

Gene: WNT4

Linked Data

• MyVariant Identifiers: chr1:g.22456185C>A (hg19) ; chr1:g.22129692C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129692C>A , CM000663.2:g.22129692C>A	GRCh38
NC_000001.10:g.22456185C>A , CM000663.1:g.22456185C>A	GRCh37
NC_000001.9:g.22328772C>A	NCBI36
NG_008974.1:g.18335G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000290167.11:c.237G>T MANE Select	ENSP00000290167.5:p.Gln79His
ENST00000290167.10:c.237G>T	ENSP00000290167.5:p.Gln79His
ENST00000415567.1:c.160G>T
ENST00000441048.1:c.72G>T	ENSP00000388925.1:p.Gln24His
NM_030761.4:c.237G>T	NP_110388.2:p.Gln79His
XM_011541597.1:c.303G>T	XP_011539899.1:p.Gln101His
XM_011541598.1:c.72G>T	XP_011539900.1:p.Gln24His
XM_011541599.1:c.303G>T	XP_011539901.1:p.Gln101His
XM_011541597.2:c.303G>T	XP_011539899.1:p.Gln101His
XM_011541598.2:c.72G>T	XP_011539900.1:p.Gln24His
NM_030761.5:c.237G>T MANE Select	NP_110388.2:p.Gln79His